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FDA 510(k)

CANDELA LASSER SYSTEMS MODIFIED

K-Number: K924158 · 1993-01-15

ApplicantCandela Laser Corp.
Decision Date1993-01-15
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CANDELA LASSER SYSTEMS MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Candela Laser Corp.. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K924158. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANDELA LASSER SYSTEMS MODIFIED?

CANDELA LASSER SYSTEMS MODIFIED is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Candela Laser Corp.. The 510(k) number is K924158.

When did CANDELA LASSER SYSTEMS MODIFIED receive FDA 510(k) clearance?

CANDELA LASSER SYSTEMS MODIFIED received FDA 510(k) clearance on 1993-01-15, under 510(k) number K924158.

Who is the listed applicant for CANDELA LASSER SYSTEMS MODIFIED?

The FDA 510(k) record lists Candela Laser Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANDELA LASSER SYSTEMS MODIFIED?

The FDA product code for CANDELA LASSER SYSTEMS MODIFIED is GEX. This falls under the Gastroenterology category.

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Other records listing Candela Laser Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K951033ANDELA DYNAMIC COOLING DEVICEK955662CANDELA Q-SWITCHED ALEXANDRITE LASERSK955011CANDELA HCS 2000 URETHERAL WARMER CATHETERK954872CANDELA CRYO-PROBE HOLDERK954934CANDELA SPTL LONG PULSE/TUNABLE PULSED DYE LASEK953412CANDELA MODEL PLTL-1 LASER SYSTEM

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Related Devices (Code: GEX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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